CN107233802B - Polyvinyl alcohol/nano silicon dioxide-titanium hybrid membrane and preparation method thereof - Google Patents
Polyvinyl alcohol/nano silicon dioxide-titanium hybrid membrane and preparation method thereof Download PDFInfo
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- CN107233802B CN107233802B CN201710441830.1A CN201710441830A CN107233802B CN 107233802 B CN107233802 B CN 107233802B CN 201710441830 A CN201710441830 A CN 201710441830A CN 107233802 B CN107233802 B CN 107233802B
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Abstract
A polyvinyl alcohol/nano silicon dioxide-titanium hybrid film is composed of polyvinyl alcohol, silicon dioxide colloid and titanium dioxide colloid, wherein the molar ratio of the silicon dioxide colloid to the titanium dioxide colloid is 1: 0.5-1.5, and the mass ratio of the mixture of the silicon dioxide colloid and the titanium dioxide colloid to the polyvinyl alcohol is 0.1-0.30: 1. According to the invention, the titanium dioxide-silica colloidal inorganic material is added into the polyvinyl alcohol organic solution, so that the mechanical property of the film can be effectively improved, the structure is stable and compact, the organic phase and the inorganic phase are compatible with each other due to the addition of the silane coupling agent, and the stability of the film is improved. The obtained hybrid membrane has the mechanical strength of 32.26-55.93 MPa, the elongation at break of 70.61-110.12%, the water swelling degree of 86.82-112.23%, the ion exchange capacity of 0.22-0.25 meq/g and the thermal decomposition temperature of 252-260 ℃.
Description
Technical Field
The invention belongs to the field of preparation of organic-inorganic ion exchange membranes, and particularly relates to a polyvinyl alcohol/nano silicon dioxide-titanium hybrid membrane and a preparation method thereof.
Background
The polyvinyl alcohol PVA is a water-soluble resin, is cheap and easy to obtain, has good film forming property and biocompatibility, and has higher hydrophilicity, oil resistance and solvent resistance. Therefore, the PVA film has wide application research in the aspects of pervaporation, reverse osmosis, ultrafiltration and the like.
TiO2Because of its advantages of good hydrophilicity, chemical stability, non-toxicity, self-cleaning property, low price, etc., it is widely used to improve the performance of membrane materials in recent years. Adding TiO into the mixture2The research on filling the surface of the film is also very much, namely, the surface of a filling material on the surface of the film contains carboxyl, carbonyl, sulfonic group, amino and other groups, so that the mechanical property and the water resistance of the film are enhanced.
Nano SiO2Is a commonly used inorganic nanoparticle, SiO2The surface of the material has high surface chemical energy and high hydrophilicity, and the surface of the material contains hydroxyl functional groups, so that the material has high functionality on the aspects of improving the corrosion resistance, oxidation resistance and chemical property stability of the material.
Journal of Applied Polymer Science 2004, 94 volume 1304-1315, reports that PVA and TEOS are used as raw materials to prepare a series of hybrid membranes through sol-gel reaction, and the hybrid membranes are Applied to a mixed solution of water and isopropanol separated by a Pervaporation (PV) method to obtain a good separation effect. In the method for preparing the hybrid membrane, silane is introduced into the organic polymer main body in the form of small molecules, so that the phenomenon of phase separation of an organic phase and an inorganic phase often exists, and the stability of the membrane is insufficient.
Journal of chemical engineering, 2007, 25 volumes, 29 pages to 32 pages, report on the use of nano TiO2The particle is filled and modified to prepare the novel TiO2The PVA hybrid membrane is applied to research of ethanol dehydration by pervaporation. Experiments show that the permeation flux is dependent on TiO2The amount increases and the separation factor decreases with increasing temperature and water mass fraction. Addition of TiO alone2The permeation flux of the filled and modified PVA film is improved, and the thermal stability is slightly insufficient.
Disclosure of Invention
In order to solve the defect of insufficient stability of an organic-inorganic ion exchange membrane in the prior art, the invention provides a polyvinyl alcohol/nano silicon dioxide-titanium hybrid membrane and a preparation method thereof.
A polyvinyl alcohol/nano silicon dioxide-titanium hybrid membrane is composed of polyvinyl alcohol, silicon dioxide colloid and titanium dioxide colloid, wherein the molar ratio of the silicon dioxide colloid to the titanium dioxide colloid is 1: 0.5-1.5, and the mass ratio of the mixture of the silicon dioxide colloid and the titanium dioxide colloid to the polyvinyl alcohol is 0.1-0.30: 1.
A preparation method of a polyvinyl alcohol/nano silicon dioxide-titanium hybrid membrane comprises the following steps:
1) preparation of polyvinyl alcohol solution
Placing polyvinyl alcohol with the hydrolysis degree of 98-99% and the average polymerization degree of 1750 +/-50 in distilled water, soaking for one day, stirring and heating to 100 ℃ at the speed of 8 ℃/h, keeping the temperature at 100 ℃ for 2.5-3 h, and preparing a polyvinyl alcohol solution with the mass fraction of 5-10%;
2) preparation of inorganic silica-titanium sols
Stirring and mixing ethanol and ethyl orthosilicate according to the mass ratio of 5: 1, dripping hydrochloric acid with the mass concentration of 3-5% under the condition of heating and stirring, and hydrolyzing for 3 hours at the temperature of 50-80 ℃ to obtain silicon dioxide colloid;
adding butyl titanate into an absolute ethyl alcohol aqueous solution according to the mass ratio of 1: 3-5 at the temperature of 60 ℃ to form a solution A, and preparing an ethyl alcohol solution B with the volume fraction of 40% -55% and the pH value of 3-4;
dropwise adding the solution A into the solution B at room temperature, violently stirring for 2.5h to completely hydrolyze butyl titanate to obtain light yellow sol, and then drying at 80 ℃ for 12h to form titanium dioxide colloid;
stirring a mixed solution of two kinds of colloids according to the molar ratio of the silicon dioxide colloid to the titanium dioxide colloid of 1: 0.5-1.5 at room temperature for 3-5 h to obtain inorganic silicon-titanium sol;
3) preparation of casting solution and film formation
According to the mass ratio of the inorganic silicon-titanium sol to the polyvinyl alcohol solution of 0.10-0.30: 1, slowly adding the inorganic silicon-titanium sol solution into the polyvinyl alcohol solution, stirring for 2 hours at room temperature, standing, vacuum filtering and defoaming to obtain a casting solution, coating the obtained casting solution on a clean support, ventilating and drying for 1-2 days at room temperature to form a film, then placing the film in a sulfuric acid aqueous solution with the mass concentration of 20-98% for crosslinking for 24 hours, washing the film with deionized water to be neutral, neutralizing with 1mol/L HCl and 1mol/L NaOH respectively, and soaking the finished film in the deionized water for later use.
Further, in the step 2), a silane coupling agent modifier is added when the mixed solution of the two colloids according to the molar ratio of the silicon dioxide colloid to the titanium dioxide colloid of 1: 0.5-1.5 is stirred for 3-5 hours at room temperature, wherein the mass ratio of the silane coupling agent modifier to the ethyl orthosilicate is 0.01-010: 1.
Further, the silane coupling agent is gamma-aminopropyltriethoxysilane (abbreviated as KH-550) or gamma- (methacryloyloxy) propyltrimethoxysilane (abbreviated as KH-570) containing an amino group.
Further, the support body in the step 3) is a glass plate, a tetrafluoroethylene plate, alumina ceramic, silicon dioxide ceramic, titanium dioxide ceramic, non-woven fabric, polyester fabric, nylon fabric or glass fiber fabric.
Further, the drying in the step 3) is vacuum drying, convection drying, conduction drying, ultraviolet drying, infrared drying, microwave drying or mechanical dehydration drying.
Further, the coating mode in the step 3) is a flowing coating mode, a dipping coating mode, a spraying coating mode, a scraping coating mode or a rotating coating mode.
The organic/inorganic hybrid membrane is formed by introducing an inorganic component into an organic matrix. On one hand, the thermal stability and solvent resistance of the inorganic membrane component can be improved, so that the mechanical strength of the membrane is improved, and on the other hand, the flexibility and film forming property of the membrane can be improved and controlled by modifying the pore structure of the membrane through the organic component. The research of the novel separation membrane obtained by combining the inorganic component and the organic material through different acting forces overcomes the defect of single component and develops a hybrid membrane with new performance, and the research becomes one of the development trends in the fields of high polymer material science, membrane material preparation and the like.
Has the advantages that:
the titanium dioxide-silica colloidal inorganic material is added into the PVA organic solution, so that the mechanical property of the membrane can be effectively improved, the structure is stable and compact, the organic phase and the inorganic phase are compatible and improved due to the addition of the silane coupling agent, and the stability of the membrane is improved. The obtained hybrid membrane has the mechanical strength of 32.26-55.93 MPa, the elongation at break of 70.61-110.12%, the water swelling degree of 86.82-112.23%, the ion exchange capacity of 0.22-0.25 meq/g and the thermal decomposition temperature of 252-260 ℃.
Drawings
FIG. 1 is a photograph of an air-side surface field emission electron microscope of a hybrid membrane prepared in example 1 of the present invention;
FIG. 2 is a cross-sectional field emission electron micrograph of the hybrid membrane prepared in example 2 of the present invention.
Detailed Description
Example 1
5g of PVA with the hydrolysis degree of 98-99% and the average polymerization degree of 1750 +/-50 is soaked in 95ml of distilled water, the mixture is placed in a stirrer after one day and stirred, the temperature is raised to 100 ℃ at the speed of 8 ℃/h and is kept for 3h to completely dissolve the PVA, and 5% PVA solution is prepared. 0.056g TEOS and 0.3ml ethanol are mixed at room temperature, 0.2ml hydrochloric acid with 3 percent mass concentration is dropped into the mixture and is hydrolyzed for 3 hours under the condition of vigorous stirring at 60 ℃ to obtain the silica sol. 3.4mL of butyl titanate was mixed with 13.6mL of absolute ethanol and stirred to form solution A. then, 3.4mL of deionized water and 3.4mL of absolute ethanol were mixed and about 0.68mL of hydrochloric acid was added dropwise, the pH was maintained at about 3-4 using a pH meter, to form solution B. Then, the solution a was added dropwise to the prepared solution B at room temperature. Meanwhile, a constant-temperature magnetic stirrer is used for carrying out violent stirring to hydrolyze the butyl phthalate. Stirring for about 3h to obtain yellowish transparent sol. Next, the resulting sol was dried in a drying oven at a temperature of 80 ℃ for 24h, finally forming a gel. Adding 0.0028g of modifier silane coupling agent KH-570 into the mixed solution of the two colloids according to the proportion of silicon dioxide to titanium dioxide of 1: 0.5, and stirring for 3h under the condition of water bath at 60 ℃ to obtain inorganic silicon-titanium colloid. Slowly adding the mixed colloid into a PVA aqueous solution, stirring for 2h at room temperature under the condition of 60 ℃, standing and aging, carrying out vacuum filtration and defoaming to obtain a membrane casting solution, pouring the obtained membrane casting solution on a clean glass plate for tape casting, carrying out ventilation drying for 1-2 d at room temperature to form a membrane, placing a part of the membrane into a sulfuric acid aqueous solution with the mass concentration of 98% for crosslinking for 24h, washing the membrane to be neutral by deionized water, neutralizing by 1mol/LHCl and 1mol/L NaOH respectively, and soaking a finished membrane in the deionized water for later use. The membrane had a mechanical strength of 55.9MPa, a tensile elongation at break of 110.12%, a water swelling capacity of 86.82%, a thermal decomposition temperature of 258 ℃ and an ion exchange capacity of 0.24 meq/g.
Example 2
6g of PVA with the hydrolysis degree of 98-99% and the average polymerization degree of 1750 +/-50 is soaked in 94ml of distilled water, the mixture is placed in a stirrer after one day and stirred, the temperature is raised to 100 ℃ at the speed of 8 ℃/h and is kept for 3h to completely dissolve the PVA, and a 6% PVA solution is prepared. 0.076g TEOS and 0.35ml ethanol are mixed at room temperature, 0.30ml hydrochloric acid with the mass concentration of 4% is dropped into the mixture, and the mixture is hydrolyzed for 3 hours under the condition of vigorous stirring at the temperature of 60 ℃ to obtain the silica sol. Mixing 3.4mL of butyl titanate with 10.2mL of absolute ethyl alcohol, stirring to form a solution A, mixing 3.4mL of deionized water and 2.8mL of absolute ethyl alcohol, and dropwise adding about 0.68mL of hydrochloric acid to keep the pH value at about 3-4 by a pH meter to form a solution B. Then, the solution a was added dropwise to the prepared solution B at room temperature. Meanwhile, a constant-temperature magnetic stirrer is used for carrying out violent stirring to hydrolyze the butyl phthalate. Stirring for about 3h to obtain yellowish transparent sol. Next, the resulting sol was dried in a drying oven at a temperature of 80 ℃ for 24h, finally forming a gel. Adding 0.0015g of modifier silane coupling agent KH-570 into the mixed solution of the two colloids according to the proportion of 1: 0.75 of silicon dioxide and titanium dioxide, and stirring for 3 hours under the condition of 70 ℃ water bath to obtain inorganic silicon-titanium colloid. Slowly adding the mixed colloid into a PVA aqueous solution, stirring for 2.5h at the room temperature under the condition of 60 ℃, standing and aging, filtering and defoaming in vacuum to obtain a casting solution, pouring the obtained casting solution on a clean glass plate for casting, ventilating and drying for 1-2 d at the room temperature to form a film, placing a part of the film in a sulfuric acid aqueous solution with the mass concentration of 50% for crosslinking for 24h, washing the film to be neutral by deionized water, neutralizing by 1mol/LHCl and 1mol/L NaOH respectively, and soaking the finished film in the deionized water for later use. The membrane had a mechanical strength of 40.23MPa, a modulus of elongation at break of 98.42%, a water-swelling capacity of 88.26%, a thermal decomposition temperature of 260 ℃ and an ion exchange capacity of 0.23 meq/g.
Example 3
8g of polyvinyl alcohol with PVA hydrolysis degree of 98-99% and average polymerization degree of 1750 +/-50 is soaked in 92ml of distilled water, the polyvinyl alcohol is placed in a stirrer after one day and stirred, the temperature is raised to 100 ℃ at 8 ℃/h and is kept for 3h to completely dissolve the PVA, and 8% PVA solution is prepared. 0.096g TEOS and 0.48ml ethanol are mixed at room temperature, 0.33ml hydrochloric acid with mass concentration of 4.5% is dropped into the mixture, and the mixture is hydrolyzed for 3 hours under the condition of vigorous stirring at 60 ℃ to obtain the silica sol. Mixing 3.4mL of butyl titanate with 15.3mL of absolute ethyl alcohol, stirring to form a solution A, mixing 3.4mL of deionized water and 2.3mL of absolute ethyl alcohol, and dropwise adding about 0.68mL of hydrochloric acid to keep the pH value at about 3-4 by a pH meter to form a solution B. Then, the solution a was added dropwise to the prepared solution B at room temperature. Meanwhile, a constant-temperature magnetic stirrer is used for carrying out violent stirring to hydrolyze the butyl phthalate. Stirring for about 3h to obtain yellowish transparent sol. Next, the resulting sol was dried in a drying oven at a temperature of 80 ℃ for 24h, finally forming a gel. Adding 0.0072g of modifier silane coupling agent KH-550 into the mixed solution of the two colloids according to the proportion of 1: 1 of silicon dioxide and titanium dioxide, and stirring for 3 hours at 70 ℃ in a water bath to obtain inorganic silicon-titanium colloid. Slowly adding the mixed colloid into a PVA aqueous solution, stirring for 2.5h at the room temperature under the condition of 60 ℃, standing and aging, filtering and defoaming in vacuum to obtain a casting solution, pouring the obtained casting solution on a clean glass plate for casting, ventilating and drying for 1-2 d at the room temperature to form a film, placing a part of the film in a sulfuric acid aqueous solution with the mass concentration of 30%, crosslinking for 24h, washing with deionized water to be neutral, neutralizing with 1mol/LHCL and 1mol/L NaOH respectively, and soaking the finished film in the deionized water for later use. The membrane had a mechanical strength of 42.52MPa, an elongation at break of 83.35%, a water-swelling capacity of 92.36%, a thermal decomposition temperature of 255 ℃ and an ion exchange capacity of 0.24 meq/g.
Example 4
10g of PVA with the hydrolysis degree of 98-99 percent and the average polymerization degree of 1750 +/-50 is soaked in 90ml of distilled water, the mixture is placed in a stirrer after one day and stirred, the temperature is raised to 100 ℃ at the speed of 8 ℃/h and is kept for 3h to completely dissolve the PVA, and 10 percent PVA solution is prepared. 0.1g TEOS and 0.50ml ethanol are mixed at room temperature, 0.3ml hydrochloric acid with the mass concentration of 5 percent is dropped into the mixture, and the mixture is hydrolyzed for 3 hours under the condition of vigorous stirring at the temperature of 60 ℃ to obtain the silica sol. 3.4mL of butyl titanate was mixed with 17.0mL of absolute ethanol and stirred to form solution A. then, 3.4mL of deionized water and 4.2mL of absolute ethanol were mixed and about 0.68mL of hydrochloric acid was added dropwise, the pH was maintained at about 3-4 using a pH meter, to form solution B. Then, the solution a was added dropwise to the prepared solution B at room temperature. Meanwhile, a constant-temperature magnetic stirrer is used for carrying out violent stirring to hydrolyze the butyl phthalate. Stirring for about 3h to obtain yellowish transparent sol. Subsequently, the sol obtained was dried in a drying oven at a temperature of 80 ℃ for 24h, finally forming a gel. Adding 0.01g of modifier silane coupling agent KH-550 into the mixed solution of the two colloids according to the ratio of silicon dioxide to titanium dioxide of 1: 1.5, and stirring for 3 hours under the condition of 70 ℃ water bath to obtain inorganic silicon-titanium colloid. Slowly adding the mixed colloid into a PVA aqueous solution, stirring for 3h at room temperature under the condition of 60 ℃, standing and aging, carrying out vacuum filtration and defoaming to obtain a casting solution, pouring the obtained casting solution on a clean glass plate for tape casting, carrying out ventilation drying for 1-2 d at room temperature to form a film, placing a part of the film in a sulfuric acid aqueous solution with the mass concentration of 20% for crosslinking for 24h, washing the film to be neutral by deionized water, neutralizing the film by 1mol/LHCl and 1mol/L NaOH respectively, and soaking the finished film in the deionized water for later use. The membrane had a mechanical strength of 32.26MPa, a tensile elongation at break of 70.61%, a water swelling capacity of 112.23%, a thermal decomposition temperature of 252 ℃ and an ion exchange capacity of 0.22 meq/g.
Therefore, the polyvinyl alcohol/nano silicon dioxide-titanium hybrid membrane has good mechanical property, swelling property and separation property. The thermal decomposition temperature is also greatly improved, which shows that the thermal stability of the film is further improved. Nano SiO2/TiO2The addition proportion of the sol also has important influence on the performances, and the comprehensive comparison is that according to the weight ratio of silicon dioxide: the film-forming property of the casting solution formed by adding the solution mixed with titanium dioxide in the ratio of 1: 0.5 into 5% PVA solution is the best, figure 1 is a photograph of an air-side surface field emission electron microscope of an example 1 of the hybrid film adsorbing material of the invention, and as can be seen from the photograph, the hybrid film is compact and uniform, although tiny nano SiO can be seen2、TiO2Particles, but no significant agglomeration occurred, indicating SiO2、TiO2The dispersion is relatively uniform in the film, and PVA and SiO are shown2、TiO2Good compatibility between the components.
FIG. 2 is a photograph of a cross-sectional field emission electron microscope of an example 1 of the hybrid membrane adsorbent of the present invention, and it can be seen from FIG. 2 that the hybrid membrane has a developed pore structure, a compact structure, and nano-particles of SiO2、TiO2The film cross-section also has no significant nanoparticles dispersed in the finger-like pore structure, indicating that the added inorganic phase is well integrated with the organic phase.
Claims (4)
1. The polyvinyl alcohol/nano silicon dioxide-titanium hybrid membrane is characterized by comprising polyvinyl alcohol, silicon dioxide colloid and titanium dioxide colloid, wherein the molar ratio of the silicon dioxide colloid to the titanium dioxide colloid is 1: 0.5-1.5, and the mass ratio of the mixture of the silicon dioxide colloid and the titanium dioxide colloid to the polyvinyl alcohol is 0.1-0.30: 1;
the preparation method of the polyvinyl alcohol/nano silicon dioxide-titanium hybrid membrane comprises the following steps:
1) preparation of polyvinyl alcohol solution
Placing polyvinyl alcohol with the hydrolysis degree of 98-99% and the average polymerization degree of 1750 +/-50 in distilled water, soaking for one day, stirring and heating to 100 ℃ at the speed of 8 ℃/h, keeping the temperature at 100 ℃ for 2.5-3 h, and preparing a polyvinyl alcohol solution with the mass fraction of 5-10%;
2) preparation of inorganic silica-titanium sols
Stirring and mixing ethanol and ethyl orthosilicate according to the mass ratio of 5: 1, dripping hydrochloric acid with the mass concentration of 3-5% under the condition of heating and stirring, and hydrolyzing for 3 hours at the temperature of 50-80 ℃ to obtain silicon dioxide colloid;
adding butyl titanate into an absolute ethyl alcohol aqueous solution according to the mass ratio of 1: 3-5 at the temperature of 60 ℃ to form a solution A, and preparing an ethyl alcohol solution B with the volume fraction of 40% -55% and the pH value of 3-4;
dropwise adding the solution A into the solution B at room temperature, violently stirring for 2.5h to completely hydrolyze butyl titanate to obtain light yellow sol, and then drying at 80 ℃ for 12h to form titanium dioxide colloid;
stirring a mixed solution of two kinds of colloids according to the molar ratio of the silicon dioxide colloid to the titanium dioxide colloid of 1: 0.5-1.5 at room temperature for 3-5 h to obtain inorganic silicon-titanium sol;
3) preparation of casting solution and film formation
Slowly adding inorganic silicon-titanium sol solution into polyvinyl alcohol solution according to the mass ratio of the inorganic silicon-titanium sol solution to the polyvinyl alcohol solution of 0.10-0.30: 1, stirring for 2 hours at room temperature, standing, filtering and defoaming in vacuum to obtain a casting solution, coating the obtained casting solution on a clean support, ventilating and drying for 1-2 days at room temperature to form a film, then placing the film in a sulfuric acid aqueous solution with the mass concentration of 20-98% for crosslinking for 24 hours, washing the film with deionized water to be neutral, neutralizing with 1mol/L HCl and 1mol/L NaOH respectively, and soaking the finished film in the deionized water for later use;
in the step 2), a silane coupling agent is added when a mixed solution of two kinds of colloids according to the molar ratio of the silicon dioxide colloid to the titanium dioxide colloid of 1: 0.5-1.5 is stirred for 3-5 hours at room temperature, wherein the mass ratio of the silane coupling agent to the tetraethoxysilane is 0.01-0.10: 1;
the silane coupling agent is gamma-aminopropyltriethoxysilane or gamma- (methacryloyloxy) propyltrimethoxysilane containing amino.
2. The polyvinyl alcohol/nano silica-titanium hybrid film according to claim 1, wherein the support in step 3) is a glass plate, a tetrafluoroethylene plate, an alumina ceramic, a silica ceramic, a titania ceramic, a non-woven fabric, a polyester fabric, a nylon fabric, or a glass fiber fabric.
3. The polyvinyl alcohol/nano-silica-titanium hybrid film according to claim 1, wherein the drying in step 3) is vacuum drying, convection drying, conduction drying, ultraviolet drying, infrared drying, microwave drying or mechanical dehydration drying.
4. The polyvinyl alcohol/nanosilica-titanium hybrid film according to claim 1, wherein the coating manner in step 3) is a flow coating, a dip coating, a spray coating, a scratch coating or a spin coating.
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| CN108715641B (en) * | 2018-05-25 | 2022-05-03 | 湖州斯蔓生物材料有限公司 | PVA hydrogel, composite material using same, method for producing same, and use thereof |
| CN109507766A (en) * | 2018-10-22 | 2019-03-22 | 西安工业大学 | In flexibility, remote dual-band infrared absorbing membrane and preparation method thereof |
| CN109821429B (en) * | 2019-03-06 | 2021-03-23 | 常州大学 | Preparation method and application of anti-pollution silicon-titanium copolymerization composite membrane |
| CN111467973B (en) * | 2020-05-27 | 2022-03-25 | 临沂大学 | Zwitterion-modified silicon-titanium hybrid nanofiltration composite membrane and preparation method thereof |
| CN115185020A (en) * | 2022-08-04 | 2022-10-14 | 江西麦帝施科技有限公司 | Diffusion medium and preparation method thereof |
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| JP2005169982A (en) * | 2003-12-15 | 2005-06-30 | Dainippon Printing Co Ltd | Shading laminated material and packaging bag using it |
| CN102029115A (en) * | 2010-10-27 | 2011-04-27 | 合肥学院 | Preparation method of ethanol pervaporation hybrid film used for removing methyl alcohol in wastewater |
| CN103849011A (en) * | 2014-03-13 | 2014-06-11 | 天津大学 | Chitosan/in-situ amphoteric silicon-titanium hybrid film as well as preparation method and application thereof |
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| JP2005169982A (en) * | 2003-12-15 | 2005-06-30 | Dainippon Printing Co Ltd | Shading laminated material and packaging bag using it |
| CN102029115A (en) * | 2010-10-27 | 2011-04-27 | 合肥学院 | Preparation method of ethanol pervaporation hybrid film used for removing methyl alcohol in wastewater |
| CN103849011A (en) * | 2014-03-13 | 2014-06-11 | 天津大学 | Chitosan/in-situ amphoteric silicon-titanium hybrid film as well as preparation method and application thereof |
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